Canonical Allele Identifier: CA403614747

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6681989A>T (hg19) ; chr19:g.6681978A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6681978A>T , CM000681.2:g.6681978A>T	GRCh38
NC_000019.9:g.6681989A>T , CM000681.1:g.6681989A>T	GRCh37
NC_000019.8:g.6632989A>T	NCBI36
NG_009557.1:g.43674T>A , LRG_27:g.43674T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2661T>A
ENST00000695653.1:c.2222T>A	ENSP00000512084.1:p.Phe741Tyr
ENST00000695654.1:c.3338T>A	ENSP00000512085.1:p.Phe1113Tyr
ENST00000695689.1:c.284T>A	ENSP00000512101.1:n.284T>A
ENST00000695690.1:n.504T>A
ENST00000695691.1:n.504T>A
ENST00000245907.11:c.4313T>A MANE Select	ENSP00000245907.4:p.Phe1438Tyr
ENST00000245907.10:c.4313T>A	ENSP00000245907.4:p.Phe1438Tyr
ENST00000596548.1:c.434T>A	ENSP00000469744.1:p.Phe145Tyr
ENST00000599899.5:n.1272T>A
ENST00000601008.1:c.242-4020T>A	ENSP00000471384.1:n.242-4020T>A
NM_000064.3:c.4313T>A	NP_000055.2:p.Phe1438Tyr
NM_000064.4:c.4313T>A MANE Select	NP_000055.2:p.Phe1438Tyr